Synthesis, crystal structure and catalytic activity in reductive amination of di-chlorido-(η(6)-p-cymene)(2'-di-cyclo-hexyl-phosphanyl-2,6-di-meth-oxy-biphen-yl-κP)ruthenium(II)

二氯-(η(6)-对异丙基甲苯)(2'-二环己基膦基-2,6-二甲氧基联苯基-κP)钌(II)的合成、晶体结构及其在还原胺化反应中的催化活性

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Abstract

The title compound, [RuCl(2)(C(10)H(14))(C(26)H(35)O(2)P)] (I), crystallizes in the monoclinic space group P2(1)/c with two crystallographically independent mol-ecules (A and B) in the asymmetric unit. The geometries of both mol-ecules are very similar and distinguished only by the twist angles of the two benzene rings in the phosphine substituents [89.54 (14) and 78.36 (14)° for mol-ecules A and B, respectively]. The Ru atoms have classical pseudo-tetra-hedral piano-stool coordination environments. The conformation of each mol-ecule is stabilized by intra-molecular C-H⋯O and C-H⋯Cl hydrogen bonds and C-H⋯π inter-actions. The two mol-ecules are linked by a C-H⋯Cl hydrogen bond. In the crystal, the mol-ecules are further linked by C-H⋯ π inter-actions, forming -A-B-A-B- chains propagating along the a-axis direction. Complex I is an active catalyst for reductive amination reaction. The catalytic activity of this complex can be explained by the lability of the p-cymene ligand, which can be replaced by two-electron ligands such as CO or amine.

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